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RU2350602C2 - Aminoalcoxyindoles, as ligands of 5-nt6 receptor, for treatment of cns diseases - Google Patents

Aminoalcoxyindoles, as ligands of 5-nt6 receptor, for treatment of cns diseases Download PDF

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RU2350602C2
RU2350602C2 RU2005121125/04A RU2005121125A RU2350602C2 RU 2350602 C2 RU2350602 C2 RU 2350602C2 RU 2005121125/04 A RU2005121125/04 A RU 2005121125/04A RU 2005121125 A RU2005121125 A RU 2005121125A RU 2350602 C2 RU2350602 C2 RU 2350602C2
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pyrrolidin
indole
ylethoxy
compound
yloxy
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Чухай ДЖАО (US)
Чухай ДЖАО
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Ф.Хоффманн-Ля Рош Аг
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Abstract

FIELD: medicine.
SUBSTANCE: in the formula I
Figure 00000080
or it pharmaceutically comprehensible salt: m it is peer 3; n it is peer from 0 to 2; all R1 independently mean H; R2 means aryl, unessentially replaced 1-2 assistants chosen from group, including halogen, and C1-C12alcoxy; R3 means H, C1-C12alkyl; p it is peer 2 or 3; R5, R6, R7 and R8 independently mean H, C1-C12alkyl, or one of R5 and R6 together with one of R7 and R8 and the atoms located between them can form a 4-7-termed heterocyclic ring, or R7 and R8 together with atom of nitrogen to which they are attached, can form a 5-7-termed heterocyclic ring; or one of R5 and R6 together with R3 and the atoms located between them can form a 5-7-termed heterocyclic ring. Bonds I possess selective opposing activity in the relation of 5-NT6 receptor.
EFFECT: possibility to use bond in a pharmaceutical composition for treatment of CNS and gastroenteric tract.
16 cl, 8 dwg, 2 tbl, 10 ex

Description

Текст описания приведен в факсимильном виде.

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The text of the description is given in facsimile form.
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Claims (16)

1. Соединение формулы I:
Figure 00000072

или его фармацевтически приемлемая соль,
в которой
m равно 3;
n равно от 0 до 2;
все R1 независимо обозначают водород;
R2 обозначает арил, необязательно замещенный 1-2 заместителями, выбранными из группы, состоящей из галогена и С1-С12алкокси;
R3 обозначает водород или С1-С12алкил;
р равно 2 или 3;
R5, R6, R7 и R8 независимо обозначают водород или С1-С12алкил, или один из R5 и R6 совместно с одним из R7 и R8 и расположенными между ними атомами могут образовать 4-7-членное гетероциклическое кольцо, или R7 и R8 совместно с атомом азота, к которому они присоединены, могут образовать 5-7-членное гетероциклическое кольцо; или один из R5 и R6 совместно с R3 и расположенными между ними атомами могут образовать 5-7-членное гетероциклическое кольцо.1. The compound of formula I:
Figure 00000072

or a pharmaceutically acceptable salt thereof,
wherein
m is 3;
n is from 0 to 2;
all R 1 are independently hydrogen;
R 2 is aryl, optionally substituted with 1-2 substituents selected from the group consisting of halogen and C 1 -C 12 alkoxy;
R 3 is hydrogen or C 1 -C 12 alkyl;
p is 2 or 3;
R 5 , R 6 , R 7 and R 8 independently represent hydrogen or C 1 -C 12 alkyl, or one of R 5 and R 6 together with one of R 7 and R 8 and the atoms located between them can form 4-7- a member heterocyclic ring, or R 7 and R 8 together with the nitrogen atom to which they are attached, can form a 5-7 membered heterocyclic ring; or one of R 5 and R 6 together with R 3 and the atoms located between them can form a 5-7 membered heterocyclic ring. 2. Соединение по п.1, в котором R2 обозначает фенил, необязательно замещенный 1-2 заместителями, выбранными из группы, состоящей из галогена и С1-С12алкокси; R5 и R6 совместно с одним из R7 и R8 и расположенными между ними атомами азота могут образовать азетидин-3-ил, пиррролидин-2-ил или пиперидин-4-ил; или R7 и R8 совместно с атомом азота, к которому они присоединены, могут образовать пирролидин-1-ил; или один из R7 и R8 совместно с R3 и расположенными между ними атомами могут образовать 6-членное гетероциклическое кольцо.2. The compound according to claim 1, in which R 2 denotes phenyl, optionally substituted with 1-2 substituents selected from the group consisting of halogen and C 1 -C 12 alkoxy; R 5 and R 6 together with one of R 7 and R 8 and the nitrogen atoms located between them can form azetidin-3-yl, pyrrolidin-2-yl or piperidin-4-yl; or R 7 and R 8 together with the nitrogen atom to which they are attached can form pyrrolidin-1-yl; or one of R 7 and R 8 together with R 3 and the atoms located between them can form a 6-membered heterocyclic ring. 3. Соединение по п.1, в котором R2 обозначает 2-галогенфенил, 3-галогенфенил, 4-галогенфенил, 2,3-дигалогенфенил, 3,4-дигалогенфенил, 2,5-дигалогенфенил, 2-С1-С12алкоксифенил или 3-С1-С12алкоксифенил.3. The compound according to claim 1, in which R 2 means 2-halogenophenyl, 3-halogenophenyl, 4-halogenophenyl, 2,3-dihalogenophenyl, 3,4-dihalogenophenyl, 2,5-dihalogenophenyl, 2-C 1 -C 12 alkoxyphenyl or 3-C 1 -C 12 alkoxyphenyl. 4. Соединение по п.3, в котором R2 обозначает 4-хлорфенил, 2,3-дихлорфенил, 2-хлорфенил, 2-фторфенил, 3-фторфенил или 2-метоксифенил.4. The compound according to claim 3, in which R 2 means 4-chlorophenyl, 2,3-dichlorophenyl, 2-chlorophenyl, 2-fluorophenyl, 3-fluorophenyl or 2-methoxyphenyl. 5. Соединение по п.1, в котором указанное соединение обладает формулой
Figure 00000073

в которой m, n, р, R1, R2, R3, R5, R6, R7 и R8 являются такими, как определено в п.1.5. The compound according to claim 1, in which the specified compound has the formula
Figure 00000073

in which m, n, p, R 1 , R 2 , R 3 , R 5 , R 6 , R 7 and R 8 are as defined in claim 1. 6. Соединение по п.5, в котором указанное соединение обладает формулой
Figure 00000074

в которой
m, р, R1, R3, R5, R6, R7 и R8 являются такими, как определено в п.1;
q равно от 0 до 2; и
все R9 независимо обозначают галоген или С1-С12алкокси.6. The compound according to claim 5, in which the specified compound has the formula
Figure 00000074

wherein
m, p, R 1 , R 3 , R 5 , R 6 , R 7 and R 8 are as defined in claim 1;
q is from 0 to 2; and
all R 9 are independently halogen or C 1 -C 12 alkoxy. 7. Соединение по п.6, в котором указанное соединение обладает формулой
Figure 00000075

в которой
m, р, R1, R3, R5, R6, R7 и R8 являются такими, как определено в п.1;
q равно от 0 до 2; и
все R9 независимо обозначают галоген или С1-С12алкокси.7. The compound according to claim 6, in which the specified compound has the formula
Figure 00000075

wherein
m, p, R 1 , R 3 , R 5 , R 6 , R 7 and R 8 are as defined in claim 1;
q is from 0 to 2; and
all R 9 are independently halogen or C 1 -C 12 alkoxy. 8. Соединение по п.6, в котором указанное соединение обладает формулой
Figure 00000076

в которой
m, p, R1, R3, R5, R6, R7 и R8 являются такими, как определено в п.1;
q равно от 0 до 2; и
все R9 независимо обозначают галоген или С1-С12алкокси.8. The compound according to claim 6, in which the specified compound has the formula
Figure 00000076

wherein
m, p, R 1 , R 3 , R 5 , R 6 , R 7 and R 8 are as defined in claim 1;
q is from 0 to 2; and
all R 9 are independently halogen or C 1 -C 12 alkoxy. 9. Соединение по п.1, в котором указанное соединение обладает формулой
Figure 00000077

в которой m, n, p, R1, R2, R3, R5, R6, R7 и R8 являются такими, как определено в п.1.9. The compound according to claim 1, in which the specified compound has the formula
Figure 00000077

in which m, n, p, R 1 , R 2 , R 3 , R 5 , R 6 , R 7 and R 8 are as defined in claim 1. 10. Соединение по п.1, в котором указанное соединение обладает формулой
Figure 00000078

в которой
m, p, R1, R3, R5, R6, R7 и R8 являются такими, как определено в п.1;
q равно от 0 до 2; и
все R9 независимо обозначают галоген или С1-С12алкокси.10. The compound according to claim 1, in which the specified compound has the formula
Figure 00000078

wherein
m, p, R 1 , R 3 , R 5 , R 6 , R 7 and R 8 are as defined in claim 1;
q is from 0 to 2; and
all R 9 are independently halogen or C 1 -C 12 alkoxy. 11. Соединение по п.10, в котором указанное соединение обладает формулой
Figure 00000079

в которой
m, р, R1, R3, R5, R6, R7 и R8 являются такими, как определено в п.1;
q равно от 0 до 2; и
все R9 независимо обозначают галоген или С1-С12алкокси.11. The compound of claim 10, wherein said compound has the formula
Figure 00000079

wherein
m, p, R 1 , R 3 , R 5 , R 6 , R 7 and R 8 are as defined in claim 1;
q is from 0 to 2; and
all R 9 are independently halogen or C 1 -C 12 alkoxy. 12. Соединение по п.1, причем указанное соединение выбрано из группы, включающей:
3-фенилсульфанил-7-(2-пирролидин-1-илэтокси)-1Н-индол;
3-бензолсульфонил-7-(2-пирролидин-1-илэтокси)-1Н-индол;
3-(3-хлорбензолсульфонил)-7-(2-пирролидин-1-илэтокси)-1Н-индол;
3-(4-хлорбензолсульфонил)-7-(2-пирролидин-1-илэтокси)-1Н-индол;
3-(2,3-дихлорбензолсульфонил)-7-(2-пирролидин-1-илэтокси)-1Н-индол;
3-(2-хлорбензолсульфонил)-7-(2-пирролидин-1-илэтокси)-1Н-индол;
3-(3,4-дихлорбензолсульфонил)-7-(2-пирролидин-1-илэтокси)-1Н-индол;
3-(2-фторбензолсульфонил)-7-(2-пирролидин-1-илэтокси)-1Н-индол;
3-(3-фторбензолсульфонил)-7-(2-пирролидин-1-илэтокси)-1Н-индол;
3-(3-метоксибензолсульфонил)-7-(2-пирролидин-1-илэтокси)-1Н-индол;
3-(2-метоксибензолсульфонил)-7-(2-пирролидин-1-илэтокси)-1Н-индол;
[2-(3-бензолсульфонил-1Н-индол-7-илокси)этил]диметиламин;
{2-[3-(2-метоксибензолсульфонил)-1Н-индол-7-илокси]этил}диметиламин;
{2-[3-(2-фторбензолсульфонил)-1Н-индол-7-илокси]этил}диметиламин;
{2-[3-(2-фторбензолсульфонил)-1Н-индол-7-илокси]этил} метиламин;
[2-(3-бензолсульфонил-1Н-индол-7-илокси)этил]метиламин;
2-(3-бензолсульфонил-1-метил-1Н-индол-7-илокси)этил]метиламин;
(S)-3-(2-фторбензолсульфонил)-7-(пирролидин-2-илметокси)-1Н-индол;
3-бензолсульфонил-7-(пиперидин-4-илокси)-1Н-индол;
[2-(2-бензолсульфонил-1Н-индол-4-илокси)этил]метиламин;
[2-(2-бензолсульфонил-1Н-индол-7-илокси)этил]метиламин;
3-(2,5-дихлорбензолсульфонил)-7-(2-пирролидин-1-илэтокси)-1Н-индол;
2-бензолсульфонил-4-(2-пирролидин-1-илэтокси)-1Н-индол;
4-(азетидин-3-илметокси)-2-бензолсульфонил-1Н-индол;
2-[3-(2-фторбензолсульфонил)-1Н-индол-7-илокси]этиламин и 1-(2-фторбензолсульфонил)-3,4-дигидро-5-окса-2а-азааценафтилен-3-иламин.12. The compound according to claim 1, wherein said compound is selected from the group consisting of:
3-phenylsulfanyl-7- (2-pyrrolidin-1-ylethoxy) -1H-indole;
3-benzenesulfonyl-7- (2-pyrrolidin-1-ylethoxy) -1H-indole;
3- (3-chlorobenzenesulfonyl) -7- (2-pyrrolidin-1-ylethoxy) -1H-indole;
3- (4-chlorobenzenesulfonyl) -7- (2-pyrrolidin-1-ylethoxy) -1H-indole;
3- (2,3-dichlorobenzenesulfonyl) -7- (2-pyrrolidin-1-ylethoxy) -1H-indole;
3- (2-chlorobenzenesulfonyl) -7- (2-pyrrolidin-1-ylethoxy) -1H-indole;
3- (3,4-dichlorobenzenesulfonyl) -7- (2-pyrrolidin-1-ylethoxy) -1H-indole;
3- (2-fluorobenzenesulfonyl) -7- (2-pyrrolidin-1-yl-ethoxy) -1H-indole;
3- (3-fluorobenzenesulfonyl) -7- (2-pyrrolidin-1-ylethoxy) -1H-indole;
3- (3-methoxybenzenesulfonyl) -7- (2-pyrrolidin-1-ylethoxy) -1H-indole;
3- (2-methoxybenzenesulfonyl) -7- (2-pyrrolidin-1-yl-ethoxy) -1H-indole;
[2- (3-benzenesulfonyl-1H-indol-7-yloxy) ethyl] dimethylamine;
{2- [3- (2-methoxybenzenesulfonyl) -1H-indol-7-yloxy] ethyl} dimethylamine;
{2- [3- (2-fluorobenzenesulfonyl) -1H-indol-7-yloxy] ethyl} dimethylamine;
{2- [3- (2-fluorobenzenesulfonyl) -1H-indol-7-yloxy] ethyl} methylamine;
[2- (3-benzenesulfonyl-1H-indol-7-yloxy) ethyl] methylamine;
2- (3-benzenesulfonyl-1-methyl-1H-indol-7-yloxy) ethyl] methylamine;
(S) -3- (2-fluorobenzenesulfonyl) -7- (pyrrolidin-2-ylmethoxy) -1H-indole;
3-benzenesulfonyl-7- (piperidin-4-yloxy) -1H-indole;
[2- (2-benzenesulfonyl-1H-indol-4-yloxy) ethyl] methylamine;
[2- (2-benzenesulfonyl-1H-indol-7-yloxy) ethyl] methylamine;
3- (2,5-dichlorobenzenesulfonyl) -7- (2-pyrrolidin-1-ylethoxy) -1H-indole;
2-benzenesulfonyl-4- (2-pyrrolidin-1-ylethoxy) -1H-indole;
4- (azetidin-3-ylmethoxy) -2-benzenesulfonyl-1H-indole;
2- [3- (2-fluorobenzenesulfonyl) -1H-indol-7-yloxy] ethylamine and 1- (2-fluorobenzenesulfonyl) -3,4-dihydro-5-oxa-2a-azaacenaphthylene-3-ylamine. 13. Фармацевтическая композиция, обладающая селективной антагонистической активностью в отношении 5-НТ6 рецептора, включающая эффективное количество соединения по п.1 в смеси с фармацевтически приемлемым носителем.13. A pharmaceutical composition having selective antagonistic activity against a 5-HT6 receptor, comprising an effective amount of a compound according to claim 1 in a mixture with a pharmaceutically acceptable carrier. 14. Фармацевтическая композиция по п.13, предназначенная для лечения или предупреждения патологического состояния центральной нервной системы.14. The pharmaceutical composition according to item 13, designed to treat or prevent a pathological condition of the central nervous system. 15. Фармацевтическая композиция по п.14, где патологическое состояние выбрано из группы, включающей психозы, шизофрению, маниакальные депрессии, невралгические нарушения, нарушения памяти, синдром нарушения внимания, болезнь Паркинсона, боковой амиотрофический склероз, болезнь Альцгеймера и болезнь Гентингтона.15. The pharmaceutical composition according to 14, where the pathological condition is selected from the group including psychosis, schizophrenia, manic depression, neuralgic disorders, memory impairment, attention deficit disorder, Parkinson's disease, amyotrophic lateral sclerosis, Alzheimer's disease and Huntington's disease. 16. Фармацевтическая композиция по п.13, предназначенная для лечения или предупреждения заболевания желудочно-кишечного тракта. 16. The pharmaceutical composition according to item 13, intended for the treatment or prevention of diseases of the gastrointestinal tract.
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